Abstract
BackgroundThe local treatment of Ewing sarcoma of bone involves surgery, radiotherapy or both. The selection of treatment depends on the anatomical extent of the tumour, the effectiveness of the proposed treatment, its morbidity, and the expectation of cure. However, not only are there variations in the approach to local treatment between individual patients, but also between treatment centres and countries. Our aim was to explore variation in practice and develop consensus statements about local treatment.MethodsA three stage modified Delphi technique was used with international collaborators. This involved an expert panel to identify areas of controversy, an online survey of international collaborators and a consensus meeting in London, UK in June 2017. In the consensus meeting, teams of clinicians discussed the local management of selected cases and their responses were collected with electronic voting.ResultsAreas of greater or less consensus were identified. The lack of evidence underpinning different approaches was noted and areas for collaborative research became apparent.ConclusionThis has demonstrated that there is an international consensus around many aspects of the local treatment of Ewing sarcoma of bone, including the use of specialist MultiDisciplinary Team (MDT) meetings with access to all appropriate treatments. However, considerable variation remains including the use of different staging investigations, decision making, definitions of response, and radiotherapy doses and timing. Further collaborative work should be undertaken to determine the impact of these variations in order to define best practice.
Highlights
The local treatment of Ewing sarcoma of bone involves surgery, radiotherapy or both
Ewing sarcoma is the second most common primary bone tumour occurring in children and young adults, with an incidence of approximately 1 per million
Ewing sarcoma can occur in any bone, with a distribution reflecting the mass of bone in the skeleton [2]
Summary
The local treatment of Ewing sarcoma of bone involves surgery, radiotherapy or both. Are there variations in the approach to local treatment between individual patients, and between treatment centres and countries. Our aim was to explore variation in practice and develop consensus statements about local treatment. Ewing sarcoma is the second most common primary bone tumour occurring in children and young adults, with an incidence of approximately 1 per million. It typically occurs in the second and third decades of life, with. Ewing sarcoma of bone classically presents with pain and an extra-osseous mass arising from the affected bone. Most cases demonstrate a translocation involving chromosomes 11 and 22 [3]
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